Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.
- NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_assertion description "[A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.
- NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_assertion evidence source_evidence_literature NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.
- NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_assertion SIO_000772 12615648 NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.
- NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_assertion wasDerivedFrom befree-20140225 NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.
- NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_assertion wasGeneratedBy ECO_0000203 NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP903705.RAhFfhW6C8skDpAUelzt9P7yTWM6N-sEQ2KLbDwhKajxw130_provenance.